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Thrombosis Journal|January 9, 2023
Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiencyHan-Lu Wang, Dan-Dan Ruan, Min Wu, et al.
Pediatric Rheumatology Online Journal|October 23, 2023
Potential regulatory role of the Nrf2/HMGB1/TLR4/NF-κB signaling pathway in lupus nephritisShi-Jie Li, Dan-Dan Ruan, Wei-Zhen Wu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 18, 2024
A novel stoploss mutation CYB5R3 c.906A>G(p.*302Trpext*42) involved in the pathogenesis of hereditary methemoglobinemiaKai-Ying He, Hong-Ping Yu, Jing Zou, et al.
BMC Cardiovascular Disorders|September 30, 2025
A novel NOTCH1 nonsense variant in a bicuspid aortic valve family with intrafamilial clinical heterogeneityQian Chen, Zi-Yan Xu, Wu Chi, et al.
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